Canonical Allele Identifier: PA105632
Gene: PAH HGNC NCBI

Linked Data

ClinVar Variation Id: 102680
ClinVar RCV Id: RCV000088928 RCV001053534 RCV003894944
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000268.1:p.Gly148Ser
CA229551
NM_000277.3:c.442G>A